HAUS2 HAUS augmin like complex subunit 2

Information
Symbol
HAUS2
Type
protein-coding
Description
HAUS augmin like complex subunit 2
Entrez Gene ID
55142
Genome
hg19
Position
chr15:42,841,036-42,862,192
Genome
hg38
Position
chr15:42,548,838-42,569,994
MIM
613429 OMIM
HGNC
HGNC:25530 HGNC
Ensembl
ENSG00000137814 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 26
Ranking
ClinVar
0
0
0
28
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM C15orf25
SYNONYM CEP27
SYNONYM HsT17025
MIM 613429 OMIM
HGNC HGNC:25530 HGNC
Ensembl ENSG00000137814 Ensembl
AllianceGenome HGNC:25530
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000568846.6 hg38 chr15 42,548,834 42,561,687 12,854
ENST00000260372.8 hg38 chr15 42,548,838 42,569,994 21,157
ENST00000568876.5 hg38 chr15 42,548,828 42,567,858 19,031
ENST00000568876.5 hg19 chr15 42,841,026 42,860,056 19,031
ENST00000568846.6 hg19 chr15 42,841,032 42,853,885 12,854
ENST00000260372.8 hg19 chr15 42,841,036 42,862,192 21,157
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